Halophenols
Medchemexpress LLC PF-00356231 hydrochloride | 820223-77-6 | 99.5% | 464.96 | 25 MG
PF-00356231 hydrochloride is a specific, non-peptidic, non-zinc chelating ligand and inhibitor of matrix metalloproteinase MMP-12 (IC50=1.4 μM). It forms a complex with MMP-12 and also demonstrates potency against MMP-13, MMP-8, MMP-9, and MMP-3.
- Specific inhibitor of MMP-12
- Non-peptidic, non-zinc chelating ligand
- Potent against MMP-13, MMP-8, MMP-9, and MMP-3
- For research use only
Medchemexpress LLC Ethylhexadecyldimeth 100g
Ethylhexadecyldimethylammonium (EHDA) bromide a surfactant has been used in a number of adsorptive separational methods such as the removal of nickel zinc and chromium ions Ethylhexadecyldimethylammonium (EHDA) bromide also can be used to prepare dye of staining intracellular ions[1][2]
Medchemexpress LLC Ethylhexadecyldimeth 500g
Ethylhexadecyldimethylammonium (EHDA) bromide a surfactant has been used in a number of adsorptive separational methods such as the removal of nickel zinc and chromium ions Ethylhexadecyldimethylammonium (EHDA) bromide also can be used to prepare dye of staining intracellular ions[1][2]
Medchemexpress LLC 5-Bromo-2-iodopyridine | 223463-13-6 | 283.89 | 50 G
5-Bromo-2-iodopyridine is a pyridine derivative containing bromine and iodine. It can be used in the synthesis of other active compounds, such as Lonafarnib. It can also react with active zinc under mild conditions to form 5-bromo-2-pyridylzinc iodide, which is utilized in various coupling reactions to obtain corresponding cross-coupling products.
- Pyridine derivative containing bromine and iodine
- Used in the synthesis of active compounds like Lonafarnib
- Reacts with active zinc to form 5-bromo-2-pyridylzinc iodide
- Utilized in various coupling reactions
Medchemexpress LLC PF-00356231 hydrochloride | 820223-77-6 | 99.0% | 464.96 | 50 MG
PF-00356231 hydrochloride is a specific, non-peptidic, non-zinc chelating ligand and inhibitor of matrix metalloproteinase MMP-12. It binds to MMP-12, forming a complex and shows potency against MMP-13, MMP-8, MMP-9, and MMP-3. Its activity can be significantly influenced by the presence of acetohydroxamate (AH).
- Specific, non-peptidic, non-zinc chelating ligand
- Inhibitor of matrix metalloproteinase MMP-12
- Potent against MMP-13, MMP-8, MMP-9, and MMP-3
- Activity affected by acetohydroxamate (AH)
Medchemexpress LLC Abametapir | 1762-34-1 | 184.24 | 25 G
Abametapir is a metalloproteinase (MMP) inhibitor that targets metalloproteinases crucial for egg hatching and louse development. It can inhibit the hatching of both head and body lice. Abametapir is also capable of chelating heavy metal ions such as iron, copper, and zinc, allowing it to interact with various insect targets that require metal co-factors for their function, including metalloproteinases.
- Inhibits metalloproteinases critical for egg hatching and louse development.
- Effective against both head and body lice.
- Chelates heavy metal ions like iron, copper, and zinc.
- Interacts with insect targets requiring metal co-factors.
Medchemexpress LLC PF-00356231 hydrochloride | 820223-77-6 | 99.0% | 464.96 | 100 MG
PF-00356231 hydrochloride is a specific, non-peptidic, non-zinc chelating ligand and inhibitor of matrix metalloproteinase MMP-12 (IC50=1.4 μM). It binds to MMP-12, forming a PF-00356231/MMP-12 complex. This compound also demonstrates potency against MMP-13, MMP-8, MMP-9, and MMP-3 with IC50 values of 0.00065, 1.7, 0.98, and 0.39 μM, respectively. It is intended for research use only.
- Specific inhibitor of matrix metalloproteinase MMP-12.
- Non-peptidic and non-zinc chelating ligand.
- Potency against MMP-13, MMP-8, MMP-9, and MMP-3.
- Available in solid and solution forms.
- Can be stored at 4°C (sealed, away from moisture) or -80°C/-20°C in solvent.
Medchemexpress LLC Abametapir | 1762-34-1 | 184.24 | 100 G
Abametapir is a metalloproteinase (MMP) inhibitor that targets metalloproteinases crucial for egg hatching and louse development. It can inhibit the hatching of both head and body lice.
- Targets metalloproteinases critical for egg hatching and louse development.
- Inhibits the hatching of head and body lice.
- Chelates heavy metal ions such as iron, copper, and zinc.
- Interacts with insect targets that require metal co-factors for function.
Medchemexpress LLC Ditiocarb sodium (Sodium diethyldithiocarbamate) | 148-18-5 | MFCD00066667 | 99.2% | 5 G
Ditiocarb sodium is an orally active copper reagent that exhibits various activities including antioxidation, chelation, anti-tumor effects, immunomodulation, and anti-HIV properties. It is suitable for research in tumors, inflammatory, and immune-related diseases.
- Acts as an accelerator in the cementation of copper from copper sulfate solution on zinc by forming a copper diethyldithiocarbamate complex.
- Inhibits Cisplatin-induced nephrotoxicity and gastrointestinal toxicity in rats.
- Exhibits antitumor activity in a mouse skin tumor model.
Medchemexpress LLC Salicylaldoxime | 94-67-7 | 99.8% | 100 G
Salicylaldoxime is an organic compound that serves as a reagent for the gravimetric determination and separation of various heavy metals such as copper, nickel, palladium, lead, bismuth, and zinc. Its copper complex has also been shown to exhibit anticancer activity, specifically inhibiting topoisomerase II and L1210 leukemia cell proliferation.
- Used as a reagent for gravimetric determination and separation of heavy metals.
- Copper complex exhibits anticancer activity.
- Inhibits topoisomerase II relaxation activity when complexed with copper.
- Inhibits L1210 leukemia cell proliferation.
Medchemexpress LLC Salicylaldoxime | 94-67-7 | 99.8% | 25 G
Salicylaldoxime is an organic compound that has been used as a reagent for the gravimetric determination and separation of Copper, Nickel, Palladium, Lead, Bismuth, and Zinc. The copper complex of Salicylaldoxime exhibits anticancer activity, completely inhibiting the relaxation activity of topoisomerase II when forming a complex with copper, and also inhibiting L1210 leukemia cell proliferation.
- Used as a reagent for gravimetric determination
- Separates various heavy metals including Copper, Nickel, and Lead
- Copper complex shows anticancer activity
- Inhibits topoisomerase II activity when complexed with copper
- Inhibits L1210 leukemia cell proliferation
Medchemexpress LLC PF-00356231 hydrochloride | 820223-77-6 | 99.5% | 464.96 | 10MM/1ML
PF-00356231 hydrochloride is a specific, non-peptidic, non-zinc chelating ligand and inhibitor of matrix metalloproteinase MMP-12 (IC50=1.4 μM). It binds to MMP-12, forming a PF-00356231/MMP-12 complex. It shows potency against MMP-13, MMP-8, MMP-9, MMP-3 with IC50s of 0.00065, 1.7, 0.98, 0.39 μM, respectively.
Features:
- MMP-12 inhibited with an IC50 of 1.4 μM
- MMP-13 inhibited with an IC50 of 0.65 nM
- MMP-3 inhibited with an IC50 of 0.39 μM
- MMP-8 inhibited with an IC50 of 1.7 μM
- MMP-9 inhibited with an IC50 of 0.98 μM
Medchemexpress LLC Carbamodithioic acid, N,N-diethyl-, sodium salt (1:1) | 148-18-5 | 99.2% | 50 G
Ditiocarb sodium is an orally active copper reagent that demonstrates various activities including antioxidation, chelation, anti-tumor effects, immunomodulation, and anti-HIV properties. It is suitable for use in research related to tumors, inflammatory, and immune-related diseases.
- Exhibits activities such as antioxidation, chelation, anti-tumor effects, immunomodulation, and anti-HIV properties.
- Can be used in the research of tumors, inflammatory, and immune-related diseases.
- Acts as an accelerator in the cementation of copper from copper sulfate solution on zinc.
- Increases the rate of copper cementation by reacting with Cu2+ solution to form a copper diethyldithiocarbamate complex.
- Can inhibit cisplatin-induced nephrotoxicity and gastrointestinal toxicity in rats.
- Exhibits antitumor activity in a mouse skin tumor model.
Medchemexpress LLC Sodium diethyldithiocarbamate | 148-18-5 | 99.2% | 1 ML
Ditiocarb sodium,98% (Sodium diethyldithiocarbamate,98%) is an orally active copper reagent that exhibits various activities such as antioxidation, chelation, anti-tumor effects, immunomodulation, and anti-HIV properties. It is suitable for research in tumors, inflammatory, and immune-related diseases.
- Orally active copper reagent.
- Exhibits antioxidation activity.
- Exhibits chelation activity.
- Exhibits anti-tumor effects.
- Exhibits immunomodulation properties.
- Exhibits anti-HIV properties.
- Can accelerate the rate of copper cementation from copper sulfate solution on zinc.
- Reacts with Cu2+ solution to form a copper diethyldithiocarbamate complex.
- Increases the rate of copper cementation, with higher concentrations leading to a more significant increase.